DK1602660T3 - Aminophosphonsyrederivater, additionssalte deraf og S1P-receptormodulatorer - Google Patents

Aminophosphonsyrederivater, additionssalte deraf og S1P-receptormodulatorer

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Publication number
DK1602660T3
DK1602660T3 DK04712184.3T DK04712184T DK1602660T3 DK 1602660 T3 DK1602660 T3 DK 1602660T3 DK 04712184 T DK04712184 T DK 04712184T DK 1602660 T3 DK1602660 T3 DK 1602660T3
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Prior art keywords
acid derivatives
receptor modulators
aminophosphonic acid
addition salts
aminophosphonic
Prior art date
Application number
DK04712184.3T
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Danish (da)
English (en)
Inventor
Yasushi Kohno
Kazuhiko Kuriyama
Wataru Hori
Kiyoaki Tanaka
Original Assignee
Kyorin Seiyaku Kk
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Publication of DK1602660T3 publication Critical patent/DK1602660T3/da

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    • C07F9/02Phosphorus compounds
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    • C07C47/00Compounds having —CHO groups
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    • C07C47/575Compounds having —CHO groups bound to carbon atoms of six—membered aromatic rings containing ether groups, groups, groups, or groups
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    • A61K31/66Phosphorus compounds
    • A61K31/661Phosphorus acids or esters thereof not having P—C bonds, e.g. fosfosal, dichlorvos, malathion or mevinphos
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    • C07C45/61Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
    • C07C45/67Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
    • C07C45/68Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
    • C07C45/70Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction with functional groups containing oxygen only in singly bound form
    • C07C45/71Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction with functional groups containing oxygen only in singly bound form being hydroxy groups
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    • C07F9/3804Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)] not used, see subgroups
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    • C07F9/3804Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)] not used, see subgroups
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    • C07F9/40Esters thereof
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  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
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  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • Engineering & Computer Science (AREA)
  • Public Health (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Biochemistry (AREA)
  • Molecular Biology (AREA)
  • Immunology (AREA)
  • Pulmonology (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Urology & Nephrology (AREA)
  • Diabetes (AREA)
  • Dermatology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Rheumatology (AREA)
  • Vascular Medicine (AREA)
  • Neurology (AREA)
  • Emergency Medicine (AREA)
  • Endocrinology (AREA)
  • Oncology (AREA)
  • Biomedical Technology (AREA)
  • Pain & Pain Management (AREA)
  • Neurosurgery (AREA)
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  • Obesity (AREA)
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DK04712184.3T 2003-02-18 2004-02-18 Aminophosphonsyrederivater, additionssalte deraf og S1P-receptormodulatorer DK1602660T3 (da)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2003039269 2003-02-18
PCT/JP2004/001783 WO2004074297A1 (ja) 2003-02-18 2004-02-18 アミノホスホン酸誘導体とその付加塩及びs1p受容体調節剤

Publications (1)

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DK1602660T3 true DK1602660T3 (da) 2011-05-23

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DK04712184.3T DK1602660T3 (da) 2003-02-18 2004-02-18 Aminophosphonsyrederivater, additionssalte deraf og S1P-receptormodulatorer

Country Status (17)

Country Link
US (2) US7456157B2 (pt)
EP (2) EP2172472B1 (pt)
JP (1) JP4564918B2 (pt)
KR (1) KR101005171B1 (pt)
CN (1) CN100344638C (pt)
AT (1) ATE504590T1 (pt)
AU (1) AU2004213297B2 (pt)
BR (1) BRPI0407658A (pt)
CA (1) CA2515574C (pt)
CY (1) CY1111529T1 (pt)
DE (1) DE602004032118D1 (pt)
DK (1) DK1602660T3 (pt)
ES (1) ES2360394T3 (pt)
MX (1) MXPA05008760A (pt)
PT (1) PT1602660E (pt)
SI (1) SI1602660T1 (pt)
WO (1) WO2004074297A1 (pt)

Families Citing this family (48)

* Cited by examiner, † Cited by third party
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EP2617711A1 (en) * 2002-09-19 2013-07-24 Kyorin Pharmaceutical Co., Ltd. Amino alcohol derivatives, salts thereof and immunosuppressive agents
KR101005171B1 (ko) * 2003-02-18 2011-01-04 교린 세이야꾸 가부시키 가이샤 아미노포스폰산 유도체와 그 부가염 및 s1p 수용체조절제
WO2005041899A2 (en) 2003-11-03 2005-05-12 University Of Virginia Patent Foundation Orally available sphingosine 1-phosphate receptor agonists and antagonists
EP1772145B1 (en) 2004-07-16 2011-03-23 Kyorin Pharmaceutical Co., Ltd. Method of effectively using medicine and method concerning prevention of side effect
US20060223866A1 (en) * 2004-08-13 2006-10-05 Praecis Pharmaceuticals, Inc. Methods and compositions for modulating sphingosine-1-phosphate (S1P) receptor activity
US7241812B2 (en) 2004-08-13 2007-07-10 Praecis Pharmaceuticals, Inc. Methods and compositions for modulating sphingosine-1-phosphate (S1P) receptor activity
JP4792400B2 (ja) * 2004-10-12 2011-10-12 杏林製薬株式会社 2−アミノ−2−[2−[4−(3−ベンジルオキシフェニルチオ)−2−クロロフェニル]エチル]−1,3−プロパンジオール塩酸塩又はその水和物の製造方法及びその製造中間体
EP1827606A2 (en) 2004-12-06 2007-09-05 University Of Virginia Patent Foundation Aryl amide sphingosine 1-phosphate analogs
PT2295049E (pt) 2005-09-09 2015-03-02 Novartis Ag Tratamento de doenças auto-imunes
WO2007043433A1 (ja) * 2005-10-07 2007-04-19 Kyorin Pharmaceutical Co., Ltd. 2-アミノ-1,3-プロパンジオール誘導体を有効成分とする肝臓疾患治療剤および肝臓疾患治療方法
AU2007209961A1 (en) 2006-01-27 2007-08-09 University Of Virginia Patent Foundation Method for treatment of neuropathic pain
TWI389683B (zh) * 2006-02-06 2013-03-21 Kyorin Seiyaku Kk A therapeutic agent for an inflammatory bowel disease or an inflammatory bowel disease treatment using a 2-amino-1,3-propanediol derivative as an active ingredient
JP2009526073A (ja) 2006-02-09 2009-07-16 ユニバーシティ オブ バージニア パテント ファンデーション 二環式スフィンゴシン−1−リン酸受容体アナログ
WO2008019090A2 (en) * 2006-08-04 2008-02-14 Praecis Pharmaceuticals Incorporated Agonists of the sphingosine-1-phosphate receptor
TWI396677B (zh) 2006-08-08 2013-05-21 Kyorin Seiyaku Kk An amine alcohol derivative and an immunosuppressive agent for use as an active ingredient
DK2058317T3 (da) 2006-08-08 2014-01-06 Kyorin Seiyaku Kk Aminophosphorsyreesterderivat og S1P receptormodulator indeholdende samme som aktiv ingrediens
EP2097397A1 (en) 2006-11-21 2009-09-09 University Of Virginia Patent Foundation Tetralin analogs having sphingosine 1-phosphate agonist activity
EP2099741A2 (en) 2006-11-21 2009-09-16 University Of Virginia Patent Foundation Hydrindane analogs having sphingosine 1-phosphate receptor agonist activity
AU2007323557A1 (en) 2006-11-21 2008-05-29 University Of Virginia Patent Foundation Benzocycloheptyl analogs having sphingosine 1-phosphate receptor activity
CA2699788C (en) 2007-10-12 2016-06-14 Novartis Ag Compositions comprising sphingosine 1 phosphate (s1p) receptor modulators
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